Clinical Trials Directory

Trials / Completed

CompletedNCT01300767

Four Week Performance Comparison Between Two Commercially Available Silicone Hydrogel Lenses

4 Week Performance Comparison Between 2 Commercially Available Silicone Hydrogel Lenses

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
75 (actual)
Sponsor
CIBA VISION · Industry
Sex
All
Age
Healthy volunteers
Not accepted

Summary

The purpose of this study is to compare the performance of two commercially marketed contact lenses when worn for up to 4 weeks in a daily wear modality.

Conditions

Interventions

TypeNameDescription
DEVICELotrafilcon B contact lens (AIR OPTIX® AQUA)Silicone hydrogel, single vision contact lens worn in one eye in a daily wear modality for approximately 5 days or more per week, at least 10 hours per day, for up to 4 weeks.
DEVICEBalafilcon A contact lens (PureVision® 2)Silicone hydrogel, single vision contact lens worn in one eye in a daily wear modality for approximately 5 days or more per week, at least 10 hours per day, for up to 4 weeks.
DEVICEContact lens solution (Clear Care®)Hydrogen peroxide-based system used for cleaning, disinfection and overnight storage of the study contact lenses.

Timeline

Start date
2011-02-01
Primary completion
2011-04-01
Completion
2011-04-01
First posted
2011-02-23
Last updated
2012-07-10
Results posted
2012-05-09

Source: ClinicalTrials.gov record NCT01300767. Inclusion in this directory is not an endorsement.